Clinical Research Associate

Roles and Responsibilities :

• Conduct site monitoring visits to ensure compliance with regulatory requirements, study protocols, and company standards.
• Collaborate with investigators, sponsors, and CROs to resolve issues related to clinical trials.
• Prepare reports on study findings, including adverse events (AEs), serious adverse events (SAEs), and other relevant data.
• Ensure timely submission of documents such as case report forms (CRFs) and query resolution letters.

Job Requirements :

• 3-5 years of experience in clinical research or a related field.
• Strong understanding of ICH-GCP guidelines and regulations governing clinical trials.
• Excellent communication skills for effective collaboration with cross-functional teams.